(Q44952429)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15218514%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

title

Analysis of the EFEMP1 gene in individuals and families with early onset drusen (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15218514%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15218514%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

Paul N. Baird

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15218514%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

author name string

Narendran N

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15218514%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

Cain M

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15218514%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

publication date

1 January 2005

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15218514%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15218514%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

volume

19

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15218514%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15218514%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

page(s)

11-15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15218514%20AND%20SRC:MED&resulttype=core&format=json

Sibling correlations and segregation analysis of age-related maculopathy: the Beaver Dam Eye Study.

30 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701435

Risk factors for age-related macular degeneration: Pooled findings from three continents.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701435

A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701435

Aberrant accumulation of EFEMP1 underlies drusen formation in Malattia Leventinese and age-related macular degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701435

Analysis of the Arg345Trp disease-associated allele of the EFEMP1 gene in individuals with early onset drusen or familial age-related macular degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701435

EFEMP1 is not associated with sporadic early onset drusen

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701435

Molecular genetic heterogeneity in autosomal dominant drusen

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701435

An overexpressed gene transcript in senescent and quiescent human fibroblasts encoding a novel protein in the epidermal growth factor-like repeat family stimulates DNA synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701435

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701435

Single-strand conformation polymorphism and heteroduplex analysis for gel-based mutation detection

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701435

How sensitive is PCR-SSCP?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701435

Pseudoexon activation in the DMD gene as a novel mechanism for Becker muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701435

Mutations in the genes encoding 11beta-hydroxysteroid dehydrogenase type 1 and hexose-6-phosphate dehydrogenase interact to cause cortisone reductase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701435

Heredity and age-related macular degeneration. Observations in monozygotic twins

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701435

inferred from DOI database lookup

7 January 2021

based on heuristic

Genetic heterogeneity in Malattia Leventinese

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701435